Standard

HDL cholesterol

LIPC · rs1077835

Where this position leads

Condition: Cholesterol (LDL, HDL and Total)

rs1077835 Condition: Cholesterol (LDL, HDL and Total) Cholesterol (LDL, HDL and Total) Condition rs1077835 rs1077835 LIPC

What each result means

A/A Two copies of the version the research linked to HDL cholesterol. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to HDL cholesterol. That is a smaller link than two copies.
G/G No copy of the version the research linked to HDL cholesterol. This is the starting point the study compared everyone against.
Source

What people read about alongside this

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs1077835

What is rs1077835?

rs1077835 is a single position in the genome, in or near the LIPC gene. Published research associates it with hdl cholesterol. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs1077835 linked to?

On MyGeneLog this position is linked to Cholesterol (LDL, HDL and Total). The research behind each link, and its sources, are set out on that condition page.

What do people read about alongside rs1077835?

Subjects that appear in the title or abstract of the same papers as this rsID include cholesterol and blood fats (1 papers), heart and circulation (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs1077835 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs1077835 come from?

GWAS Catalog, J Med Genet 2013, PMID:23505323. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

HDL cholesterol (rs1077835). MyGeneLog™. https://www.mygenelog.com/variants/rs1077835

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